4-Methylmorpholine → HCID 57980172, compound

HRID 1677140Notes

Reaction equation

HRID 1677140 reaction equation
[Na+].[C:2]([C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:19]=[CH:18][C:14]([C:15]([O-:17])=O)=[CH:13][CH:12]=2)=[N:9][CH:10]=1)(=[O:4])[CH3:3].CN1CCOCC1.ClC1N=C(OC)N=C(OC)N=1.[NH:38]1[CH2:42][CH2:41][CH2:40][C@H:39]1[CH2:43][N:44]1[CH2:48][CH2:47][CH2:46][CH2:45]1>ClCCl>[N:44]1([CH2:43][C@@H:39]2[CH2:40][CH2:41][CH2:42][N:38]2[C:15]([C:14]2[CH:13]=[CH:12][C:11]([C:8]3[N:9]=[CH:10][C:5]([C:2](=[O:4])[CH3:3])=[CH:6][CH:7]=3)=[CH:19][CH:18]=2)=[O:17])[CH2:48][CH2:47][CH2:46][CH2:45]1

Participants

6

Procedure

Procedure W′: To a stirring solution of 4-(5-acetyl-pyridin-2-yl)-benzoic acid sodium salt (1.0 mmol) and n-methyl morpholine (1.0 mmol) in dichloromethane (0.10M) in a 0° C. ice bath, add 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.0 mmol). Remove the ice bath and stir for 45 minutes. After this time, add (S)-(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (1.0 mmol) and stir at room temperature for three hours. After this time, wash the reaction with saturated aqueous sodium bicarbonate while extracting with 10% isopropanol/dichloromethane (3×). Dry the organic layer with sodium sulfate, filter and concentrate in vacuo. Purify the title compound via chromatography eluting with 2M ammonia in methanol and dichloromethane. MS (m/e): 378.3 (M+1)

Workup

  1. customRemove the ice bath
  2. stirringstir at room temperature for three hours
  3. washAfter this time, wash
  4. customthe reaction with saturated aqueous sodium bicarbonate
  5. extractionwhile extracting with 10% isopropanol/dichloromethane (3×)
  6. dry with materialDry the organic layer with sodium sulfate
  7. filtrationfilter
  8. concentrationconcentrate in vacuo
  9. customPurify the title compound via chromatography
  10. washeluting with 2M ammonia in methanol and dichloromethane

Sources & evidence

ORD record
ord-d9e3643d3d1245918c717f00e186fad8
Source dataset
uspto-grants-2011_08
Patent number
US08008301B2

Reaction notes

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